FSP Bench Clinical Research Associate I

Thermo Fisher Scientific seeks a Clinical Research Associate to monitor investigator sites, ensure data accuracy, and maintain regulatory compliance for clinical trials. The role involves on-site and remote monitoring activities, risk-based assessment, and frequent travel throughout Chile.

Responsibilities

• Monitor investigator sites using risk-based approach; conduct source data reviews and case report form verification
• Assess investigational product through physical inventory and records review at trial sites
• Document findings in reports and escalate deficiencies to clinical management for resolution
• Initiate and close out clinical trial sites; ensure essential documents meet ICH-GCP and regulatory standards
• Facilitate communication between investigative sites, client company, and internal teams; provide trial status updates

Requirements

• Bachelor's degree in life sciences or registered nursing certification
• Minimal clinical monitoring experience (~2 years) in clinical trials or related healthcare field
• Knowledge of medical terminology and clinical research protocols
• Risk-based monitoring and root cause analysis skills
• Ability to travel 60-80% or more; flexible for overnight stays
• Compliance with sponsor/client-specific requirements including potential health disclosures